697289-68-2 Usage
Chemical compound
2-Azabicyclo[2.2.2]octane-3-carboxylic acid, 5,6-dihydroxy-, ethyl ester, (1R,3S,4R,5R,6S)(9CI)
Structure
Complex structure belonging to the category of esters
Derivative
Derived from 2-Azabicyclo[2.2.2]octane-3-carboxylic acid
2-Azabicyclo[2.2.2]octane-3-carboxylic acid
Bicyclic compound with potential pharmaceutical applications
Ethyl ester derivative
Contains hydroxy groups at positions 5 and 6
Stereoisomerism
Denoted by the (1R,3S,4R,5R,6S) configuration
Potential applications
Medicinal chemistry, drug development, and biochemical research
Unique properties
Unique structure and properties
Further research
Required to fully understand its potential uses and effects.
Check Digit Verification of cas no
The CAS Registry Mumber 697289-68-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 6,9,7,2,8 and 9 respectively; the second part has 2 digits, 6 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 697289-68:
(8*6)+(7*9)+(6*7)+(5*2)+(4*8)+(3*9)+(2*6)+(1*8)=242
242 % 10 = 2
So 697289-68-2 is a valid CAS Registry Number.
697289-68-2Relevant articles and documents
2-CYANOPYRROLIDINECARBOXAMIDE COMPOUND
-
Page/Page column 38-39, (2008/06/13)
A compound of the formula (I) or a pharmaceutically acceptable salt thereof: [wherein X1 and X2 each is independently lower alkylene; X3 is =CH2, =CHF or =CF2; R1 is substituent, R2 and R3 each is independently H or lower alkyl; n is 0, 1, 2, 3 or 4.] having the activity inhibiting DPP-IV activity. They are therefore useful in the treatment of conditions mediated by DPP-IV, such as NIDDM.
Short and efficient synthesis of diazabicycloalkane dipeptide mimics
Maison, Wolfgang,Küntzer, Daniela,Grohs, Daniel
, p. 1795 - 1798 (2007/10/03)
A new synthetic route to enantiomerically pure diazabicycloalkanes is reported. Key step of this synthesis is an oxidative cleavage of azabicycloalkene precursors that are synthesized in enantiomerically pure form via aza-Diels-Alder reaction. A range of diazabicycloalkanes with different amino acid side chains have been synthesized and their structure has been elucidated by NMR analysis.
